Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g34630 | A05 | 35735247 | C | T | upstream_gene_variant | MODIFIER | c.-4129C>T| |
S216 |
2 | BAA05g34630 | A05 | 35735334 | C | T | upstream_gene_variant | MODIFIER | c.-4042C>T| |
S117 |
3 | BAA05g34630 | A05 | 35736254 | G | A | upstream_gene_variant | MODIFIER | c.-3122G>A| |
S271 |
4 | BAA05g34630 | A05 | 35739354 | C | T | upstream_gene_variant | MODIFIER | c.-22C>T| |
S233 |
5 | BAA05g34630 | A05 | 35741541 | C | T | synonymous_variant | LOW | c.939C>T|p.Tyr313Tyr |
S148 |
6 | BAA05g34630 | A05 | 35741753 | C | T | splice_region_variant&intron_variant | LOW | c.1044+7C>T| |
S182 |
7 | BAA05g34630 | A05 | 35741942 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1084-1G>A| |
S44 |
8 | BAA05g34630 | A05 | 35742085 | C | T | missense_variant | MODERATE | c.1226C>T|p.Ala409Val |
S216 |